1. Gene
  2. CAMK1D - calcium/calmodulin dependent protein kinase ID Gene

CAMK1D - calcium/calmodulin dependent protein kinase ID Gene

中文名称:钙/钙调蛋白依赖性蛋白激酶 ID

种属: Homo sapiens

同用名: CKLiK; CaM-K1; CaMKID

基因 ID: 57118 | 基因类型: protein coding

关于 CAMK1D

Cytogenetic location: 10p13 Genomic coordinates (GRCh38): 10:12,349,547-12,835,545 (from NCBI)

This gene has 3 transcripts (splice variants), 267 orthologues and 22 paralogues. Broad expression in brain (RPKM 10.9), skin (RPKM 4.6) and 21 other tissues.

功能概要

该基因是钙/钙调蛋白依赖性蛋白激酶 1 家族的成员,该家族是丝氨酸/苏氨酸激酶的一个亚家族。编码的蛋白质是钙调节的钙调蛋白依赖性蛋白激酶级联的组成部分。它与多种过程相关,包括粒细胞功能的调节、CREB 依赖性基因转录的激活、醛固酮的合成、中性粒细胞的分化和激活以及红白血病细胞的凋亡。已经描述了编码该基因的不同同种型的可变剪接转录物变体。[RefSeq 提供,2015 年 1 月]

This gene is a member of the calcium/calmodulin-dependent protein kinase 1 family, a subfamily of the serine/threonine kinases. The encoded protein is a component of the calcium-regulated calmodulin-dependent protein kinase cascade. It has been associated with multiple processes including regulation of granulocyte function, activation of CREB-dependent gene transcription, aldosterone synthesis, differentiation and activation of neutrophil cells, and Apoptosis of erythroleukemia cells. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq, Jan 2015]

CAMK1D 基因产物(3)

mRNA Protein Name
NM_001351032.2 NP_001337961.1 calcium/calmodulin-dependent protein kinase type 1D isoform 3
NM_020397.4 NP_065130.1 calcium/calmodulin-dependent protein kinase type 1D isoform 1
NM_153498.4 NP_705718.1 calcium/calmodulin-dependent protein kinase type 1D isoform 2
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables calcium/calmodulin-dependent protein kinase activity IDA
IDA: 通过直接分析推断
11050006 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
32707033 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of CREB transcription factor activity IDA
IDA: 通过直接分析推断
16324104 GOA
involved in positive regulation of phagocytosis IMP
IMP: 通过突变表型推断
15840691 GOA
involved in positive regulation of respiratory burst IMP
IMP: 通过突变表型推断
15840691 GOA
involved in regulation of dendrite development IMP
IMP: 通过突变表型推断
17056143 GOA
involved in regulation of granulocyte chemotaxis IMP
IMP: 通过突变表型推断
15840691 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
11050006 GOA
located in nucleus IDA
IDA: 通过直接分析推断
16324104 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

CAMK1D 蛋白结构

Pkinase

Pkinase: Protein kinase domain (23 - 279)

  • 0
  • 100
  • 200
  • 300
  • 385 a.a.
蛋白主名 其他名称

calcium/calmodulin-dependent protein kinase type 1D

CAMK1D/ANAPC5 fusion

CAMK1D 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
CAMK1D Q8IU85 CAMK1 Homo sapiens Q14012 32707033
种属内
CAMK1D Q8IU85 CAMK1 Homo sapiens Q14012 33961781
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 CAMK1D 蛋白

目录号 产品名 蛋白编号 纯度
HY-P7715 CAMKI delta/CAMK1D Protein, Human (GST) Q8IU85-1 (M1-K385) ≥95%

关联疾病

疾病名称 别名
Ceroid Lipofuscinosis, Neuronal, 6a

Neuronal Ceroid Lipofuscinosis 6

CLN6

Vlincl

Cln6 Disease

Ceroid Lipofuscinosis, Neuronal, 6

Late-Infantile Neuronal Ceroid Lipofuscinosis

CLN6A

Neuronal Ceroid Lipofuscinosis, Late Infantile, Variant

Neuronal Ceroid Lipofuscinosis 6a

Neuronal Ceroid Lipofuscinosis 6 Variable Age Of Onset

Cln6 Disease, Adult Kufs Type A

Cln6 Disease, Late Infantile

Neuronal Ceroid Lipofuscinosis, Gypsy/Indian Early Juvenile Variant

Ceroid Lipofuscinosis Neuronal 6

Cln6-Related Neuronal Ceroid Lipofuscinosis

Late Infantile Neuronal Ceroid Lipofuscinosis

Jansky-Bielschowsky Disease

Lincl

Late Infantile Ncl

Neuronal Ceroid Lipofuscinosis 6 With Variable Age At Onset

Variant Late-Onset Infantile Neuronal Ceroid Lipofuscinosis

Ceroid Lipofuscinosis, Neuronal, Late Infantile, Variant

Lipofuscinosis, Ceroid, Neuronal, Type 6

Ceroid Lipofuscinosis, Neuronal, 5

Wolfram Syndrome 1

WFS1

Didmoad

Wfs

Diabetes Mellitus And Insipidus With Optic Atrophy And Deafness

Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness

Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness Syndrome

Wolfram Syndrome

Type 2 Diabetes Mellitus

Insulin Resistance

NIDDM

Type 2 Diabetes

Diabetes Mellitus, Non-Insulin-Dependent

T2D

Noninsulin-Dependent Diabetes Mellitus

Diabetes Mellitus, Type Ii

Maturity-Onset Diabetes

Insulin Resistance, Severe, Digenic

Diabetes Mellitus, Type 2

Diabetes Mellitus, Noninsulin-Dependent

Diabetes Mellitus, Noninsulin-Dependent, Association With

Diabetes Mellitus, Noninsulin-Dependent, Late Onset

Hypertension, Insulin Resistance-Related, Susceptibility To

Insulin Resistance, Susceptibility To

Non-Insulin-Dependent Diabetes Mellitus

Type Ii Diabetes Mellitus

Adult-Onset Diabetes Mellitus

Maturity-Onset Diabetes Mellitus

Diabetes Mellitus Type 2

Type Ii Diabetes

Type 2 Diabetes Mellitus, Susceptibility To

Diabetes, Type 2

Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

Diabetes Mellitus, Type 2, Susceptibility To

Diabetes Mellitus, Noninsulin-Dependent, 2

Diabetes Mellitus, Type Ii, Susceptibility To

Hypertension, Insulin Resistance-Related

Adult-Onset Diabetes

Aodm

Diabetes Mellitus, Adult-Onset

Diabetes Mellitus Type Ii

Diabetes Mellitus Type 2, Susceptibility To

Diabetes, Type Ii, Susceptibility To

Diabetes Type 2

Diabetes Mellitus

Adult Onset Diabetes

Maturity Onset Diabetes

Nonketotic Diabetes

Non-Insulin Dependent Diabetes Mellitus

T2dm - [Type 2 Diabetes Mellitus]

Niddm - [Non Insulin Dependent Diabetes Mellitus]

Dm2

Dm Type Ii

Diabetic Type 2

Insulin Requiring Type 2 Diabetes

Noninsulin Dependent Diabetes

Non-Insulin-Dependent Diabetes Mellitus Without Complications

Diabetes Due To Insulin Secretory Defect

Diabetes Mellitus Due To Insulin Secretory Defect

Non-Insulin-Dependent Diabetes Of The Young

Senile Diabetes

Nonketotic Hyperglycaemia

Stable Diabetes

Diabetes Mellitus

Diabetes

Maturity-Onset Diabetes Of The Young

MODY

Maturity Onset Diabetes Mellitus In Young

Mason-Type Diabetes

Mason Type Diabetes

Maturity Onset Diabetes Of The Young

Mody Syndrome

Diabetes Of The Young, Maturity-Onset

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Mus musculus CAMK1D MGD MGI:2442190
Bos taurus CAMK1D VGNC VGNC:58595
Macaca mulatta CAMK1D VGNC VGNC:70579
Rattus norvegicus CAMK1D RGD RGD:1560691
Canis familiaris CAMK1D VGNC VGNC:38678
Felis catus CAMK1D VGNC VGNC:60329
Others CAMK1D NCBI